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Effect of Tele-Yoga Therapy on Patients With Chronic Musculoskeletal Pain During Covid-19 Lockdown

Not Applicable
Completed
Conditions
Chronic Musculoskeletal Pain
Interventions
Other: Primary care
Other: Tele-yoga therapy
Registration Number
NCT04466605
Lead Sponsor
Aarogyam UK
Brief Summary

Covid-19 outbreak and lockdown measures raised significant concerns over clinical management of chronic pain patients around the world. Patients with chronic musculoskeletal pain (CMSP) are at high risk of physical disability, psychological distress, and poor quality of life. Analgesic medications were main management during lockdown, but opioid-related concerns have prompted to find immediate alternatives.

Present study was undertaken to determine whether patients randomized to tele-yoga therapy would experience less pain, disability and improved global health, adherence and satisfaction, compared with patients assigned to usual care.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
64
Inclusion Criteria
  • Patients having pain that was musculoskeletal, defined as regional (joints, limbs, back, neck) or more generalized (fibromyalgia or chronic widespread pain);
  • Persistent pain ( ≥3 months) despite trying conventional treatment.
  • Access to virtual platform with internet.
  • Ready to give informed consent
Exclusion Criteria
  • Schizophrenia,
  • Psychiatric disorder
  • Cognitive impairment
  • Suicidal ideation
  • Current illicit drug use
  • Terminal illness

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Usual CarePrimary carePatients randomized to usual care continued to receive care for their chronic musculoskeletal pain from their primary care physician. There was no attempt by to influence clinical management unless an emergency arose
Tele-Yoga TherapyTele-yoga therapyAll patients randomized to the intervention group had one to one yoga sessions with yoga therapist twice a week for 45 minutes on secure virtual platform. Patients were encouraged with home practice to follow everyday at least for 30-mins.
Primary Outcome Measures
NameTimeMethod
Interference of painFrom baseline to 6-week post intervention

Interference of pain in 7 areas (mood, physical activity, work, social activity, relations with others, sleep, enjoyment of life) were reported using BPI

Severity of painFrom baseline to 6-week post intervention

Pain was assessed using the Brief Pain Inventory (BPI), which rates the severity of pain on 4 items (current, worst, least, and average pain in past week)

Secondary Outcome Measures
NameTimeMethod
Global rating of change in painFrom baseline to 6-week post interventiona

7-point global rating of pain change was used to assess change in pain

Intervention specific satisfactionFrom baseline to 6-week post interventiona

10 point scale was used to assess intervention-specific satisfaction

Trial Locations

Locations (1)

NMP Medical Research Institute

🇮🇳

Jaipur, Rajasthan, India

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